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Neurology
Focuses on brain health.
Sub Categories on Neurology
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Scientists discover 'entirely unanticipated' role of protein netrin1 in spinal cord development

Scientists discover 'entirely unanticipated' role of protein netrin1 in spinal cord development

by Ani Vahradyan,University of California, Los AngelesCells (blue) at the ventral midline of the spinal cord, expressing netrin1 (red) and a fluorescent tracer (GFP, green). Credit: Samantha But

Scientists discover 'entirely unanticipated' role of protein netrin1 in spinal cord development

by Ani Vahradyan,University of California, Los AngelesCells (blue) at the ventral midline of the spinal cord, expressing netrin1 (red) and a fluorescent tracer (GFP, green). Credit: Samantha But
FDA grants orphan drug designation to potential treatment of STXBP1 developmental and epileptic encephalopathy

FDA grants orphan drug designation to potential treatment of STXBP1 developmental and epileptic encephalopathy

by Graciela Gutierrez,Baylor College of MedicineDNA, which has a double-helix structure, can have many genetic mutations and variations. Credit: NIHResearch that was carried out by Baylor Colleg

FDA grants orphan drug designation to potential treatment of STXBP1 developmental and epileptic encephalopathy

by Graciela Gutierrez,Baylor College of MedicineDNA, which has a double-helix structure, can have many genetic mutations and variations. Credit: NIHResearch that was carried out by Baylor Colleg
Study shows potential of optogenetics in treating epilepsy

Study shows potential of optogenetics in treating epilepsy

byUniversity of California, San FranciscoHD-MEA recordings of human hippocampal slices. Credit:Nature Neuroscience(2024). DOI: 10.1038/s41593-024-01782-5In what could one day become

Study shows potential of optogenetics in treating epilepsy

byUniversity of California, San FranciscoHD-MEA recordings of human hippocampal slices. Credit:Nature Neuroscience(2024). DOI: 10.1038/s41593-024-01782-5In what could one day become
Scientists uncover new biallelic repeat expansion leading to mitochondrial encephalopathy

Scientists uncover new biallelic repeat expansion leading to mitochondrial encephalopathy

by Juntendo University Research Promotion CenterCredit:npj Genomic Medicine(2024). DOI: 10.1038/s41525-024-00429-5Mitochondrial diseases are among the most prevalent hereditary metabolic d

Scientists uncover new biallelic repeat expansion leading to mitochondrial encephalopathy

by Juntendo University Research Promotion CenterCredit:npj Genomic Medicine(2024). DOI: 10.1038/s41525-024-00429-5Mitochondrial diseases are among the most prevalent hereditary metabolic d
New drug targets for Alzheimer's identified from cerebrospinal fluid

New drug targets for Alzheimer's identified from cerebrospinal fluid

by Mark Reynolds,Washington University School of MedicineCellular localization of immune and lysosomal proteins. Credit:Nature Genetics(2024). DOI: 10.1038/s41588-024-01972-8A multit

New drug targets for Alzheimer's identified from cerebrospinal fluid

by Mark Reynolds,Washington University School of MedicineCellular localization of immune and lysosomal proteins. Credit:Nature Genetics(2024). DOI: 10.1038/s41588-024-01972-8A multit
Huntington's disease gene may also enhance early brain development and intelligence

Huntington's disease gene may also enhance early brain development and intelligence

by Jennifer Brown,University of IowaYears-to-onset (YTO)-dependent brain functional changes. Credit:Annals of Neurology(2024). DOI: 10.1002/ana.27046The genetic mutation that causes

Huntington's disease gene may also enhance early brain development and intelligence

by Jennifer Brown,University of IowaYears-to-onset (YTO)-dependent brain functional changes. Credit:Annals of Neurology(2024). DOI: 10.1002/ana.27046The genetic mutation that causes
New research offers hope for treating inherited peripheral neuropathies

New research offers hope for treating inherited peripheral neuropathies

by Uniformed Services University of the Health Sciences (USU)Treating S63del mice for 21 days with tadalafil or CYR119 restores myelin thickness and nerve conduction in sciatic nerves. Credit:Ce

New research offers hope for treating inherited peripheral neuropathies

by Uniformed Services University of the Health Sciences (USU)Treating S63del mice for 21 days with tadalafil or CYR119 restores myelin thickness and nerve conduction in sciatic nerves. Credit:Ce
Immune exhaustion in myalgic encephalomyelitis/chronic fatigue syndrome and long COVID

Immune exhaustion in myalgic encephalomyelitis/chronic fatigue syndrome and long COVID

byGriffith UniversityCredit: Griffith UniversityUnlocking the secrets behind immune exhaustion in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and long COVID patients is at the ce

Immune exhaustion in myalgic encephalomyelitis/chronic fatigue syndrome and long COVID

byGriffith UniversityCredit: Griffith UniversityUnlocking the secrets behind immune exhaustion in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and long COVID patients is at the ce
Researchers identify possible treatment for rare disorder CTNNB1 syndrome

Researchers identify possible treatment for rare disorder CTNNB1 syndrome

byTufts UniversityCredit:EMBO Molecular Medicine(2024). DOI: 10.1038/s44321-024-00110-5Researchers at Tufts University School of Medicine and the Graduate School of Biomedical Scienc

Researchers identify possible treatment for rare disorder CTNNB1 syndrome

byTufts UniversityCredit:EMBO Molecular Medicine(2024). DOI: 10.1038/s44321-024-00110-5Researchers at Tufts University School of Medicine and the Graduate School of Biomedical Scienc
Study confirms cognitive deficits in people with the rare disease MOGAD

Study confirms cognitive deficits in people with the rare disease MOGAD

by Stefan Zorn, Medizinische Hochschule HannoverMean z-scores of neuropsychological tests at baseline (patients <60 years). PASAT, Paced Auditory Serial Addition Task; SDMT, Symbol Digit Modalities

Study confirms cognitive deficits in people with the rare disease MOGAD

by Stefan Zorn, Medizinische Hochschule HannoverMean z-scores of neuropsychological tests at baseline (patients <60 years). PASAT, Paced Auditory Serial Addition Task; SDMT, Symbol Digit Modalities
FDA approves Miplyffa for treatment of Niemann-Pick disease, type C

FDA approves Miplyffa for treatment of Niemann-Pick disease, type C

by Lori SolomonThe U.S. Food and Drug Administration has approved Zevra Therapeutics' Miplyffa (arimoclomol), an oral medication for the treatment of Niemann-Pick disease, type C (NPC).Miplyffa, i

FDA approves Miplyffa for treatment of Niemann-Pick disease, type C

by Lori SolomonThe U.S. Food and Drug Administration has approved Zevra Therapeutics' Miplyffa (arimoclomol), an oral medication for the treatment of Niemann-Pick disease, type C (NPC).Miplyffa, i